Scroll Up
Scroll Down
Play Play Play Play
Unregistered User
Click here if this is not your Personal Edition
 
Contact Us | Free E-Mail Updates | Journals | Register a colleague
 
 
Neurologic Other
 
   
 
SEARCH   
Doctor's Guide Free CME
Medline
Congress Resource Centre
 

 EXPLORE :
   Most Read News
 All News  All News
 All Webcasts / CME  All Webcasts / CME
 All Cases  All Cases
 Congress Resource Centre  Congress Resource Centre
 All Medical Resources  All Medical Resources
 Medical  My Personal Edition



Warning | Privacy

 

 
 Recent news - Neurologic Other
    Hypertension May Predict Dementia in Older Adults With Certain Cognitive Deficits - (DGNews)
    Latrepirdine May Have Beneficial Effects in Patients With Huntington's Disease - (DGNews)
    New Tool Can Determine Need for CT Scans in Children With Minor Head Injury - (DGNews)
    Willful Modulation of Brain Activity in Disorders of Consciousness - (N Engl J Med)
    Brainstem serotonergic deficiency in sudden infant death syndrome - (JAMA)

    News archive

     Recent webcasts/CME - Neurologic Other
      Community Integration and Quality of Life Following Spinal Cord Injury
      Importance of Exercise and Nutrition Following SCI
      Prevention and Treatment of Secondary Complications after SCI
      Therapeutic Hypothermia
      Arteriovenous Malformations Dural Arteriovenous Shunts

      Webcasts/CME archive

       Recent cases - Neurologic Other
        Acute Epiglottitis As The Initial Presentation Of Pediatric Systemic Lupus Erythematosus
        Perforating Eyelid Injury Extending To The Brain Stem In A 17-Year-Old Woman: A Case Report
        Cerebral Lipiodol Embolism Following Transcatheter Arterial Chemoembolization For Hepatocellular Carcinoma
        A Migraine Variant With Abdominal Colic And Alice In Wonderland Syndrome: A Case Report And Review
        Intramedullary Non-Specific Inflammatory Lesion Of Thoracic Spine: A Case Report

        Cases archive
          




        my personal edition > neurologic other > news
        divider

          E-Mail this DGNews to a colleague

        DGNews


        Avicena Compound Receives Orphan Drug Designation for Huntington's Disease

        PALO ALTO, C.A. -- March 22, 2006 -- The Avicena Group, Inc. announced today that the United States Food and Drug Administration (FDA) has granted orphan drug designation to HD-02, the company's proprietary drug candidate for the treatment of Huntington's disease.

        The company recently announced the publication of positive Phase I/II data for HD-02 in the journal Neurology.

        The findings showed that the drug was safe and well-tolerated by patients at a dose of eight grams/day, while resulting in elevated serum and brain levels of creatine. Additional findings demonstrated that HD-02 reduced serum 8-hydroxy-2'-deoxyguanosine (serum 8OH2'dG) levels, which are markedly elevated in HD patients.

        Some researchers believe that this decrease in serum 8OH2'dG may suggest reduced oxidative injury in patients with Huntington's disease. The study's investigators intend to use the findings from this trial to design late-stage studies of HD-02 aimed at examining the drugs' ability to slow or halt the progression of Huntington's disease.

        Orphan drug designation is designed to provide developers of orphan drug products with incentives including: eligibility for seven-year marketing exclusivity following drug approval; tax credits for clinical research; reduced NDA filing fees; grants for further clinical research and development; and assistance with the review of clinical trial protocols. Additionally, orphan drug designation typically results in expedited FDA marketing review times as compared to other drugs. This is due to the fact that those conditions classified as orphan drug diseases are serious or life-threatening and afflict less than 200,000 patients annually in the U.S.

        About Huntington's Disease
        Huntington's disease is a progressive neurodegenerative disease that is caused by a defective gene. This genetic defect, which is often inherited, causes the deterioration of neurons in those parts of the brain that are responsible for controlling cognitive, emotional and motor functions. As a result, patients suffer a variety of symptoms including uncontrollable muscle movements, clumsiness, memory loss, and, ultimately, severe mental deterioration. In the United States, approximately 35,000 people suffer from Huntington's disease. There is presently no known cure for Huntington's disease.


        SOURCE: Avicena Group, Inc.



        E-Mail this DGNews to a colleague   To print, use this version






        All contents Copyright (c) 1995-2010 Doctor's Guide Publishing Limited. All rights reserved.



        The NTK initiative. Physicians helping physicians identify Need-To-Know science
           Feedback
        Please rate this article: Strongly DISAGREE...Strongly AGREE NTK logo
        Question 1 - Physicians need to become aware of this information as soon as possible. Question 2 - This information is likely to have an impact on the way physicians practice medicine.
        1
        2
        3
        4
        5
        6
        7
        Send